Canonical Allele Identifier: CA939090974
Gene: NDUFS8 HGNC NCBI

Linked Data

dbSNP Id: rs769533077

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68036622C>T , CM000673.2:g.68036622C>T GRCh38
NC_000011.9:g.67804089C>T , CM000673.1:g.67804089C>T GRCh37
NC_000011.8:g.67560665C>T NCBI36
NG_007878.1:g.2607C>T , LRG_115:g.2607C>T
NG_017040.1:g.11006C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313468.10:c.*29C>T MANE Select ENSP00000315774.5:n.*29C>T
ENST00000313468.9:c.*29C>T ENSP00000315774.5:n.*29C>T
ENST00000524810.5:c.594C>T
ENST00000528492.1:c.*29C>T ENSP00000432848.1:n.*29C>T
ENST00000531282.1:n.514C>T
NM_002496.3:c.*29C>T NP_002487.1:n.*29C>T
XM_005274013.1:c.*29C>T XP_005274070.1:n.*29C>T
XM_005274014.1:c.*29C>T XP_005274071.1:n.*29C>T
XM_005274015.1:c.*29C>T XP_005274072.1:n.*29C>T
XM_011545053.1:c.*29C>T XP_011543355.1:n.*29C>T
NM_002496.4:c.*29C>T MANE Select NP_002487.1:n.*29C>T